Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance.
- NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_assertion description "[Deficiency of X-linked inhibitor of apoptosis (XIAP), caused by BIRC4 gene mutations, is the second known cause of X-linked lymphoproliferative disease (XLP), a rare primary immunodeficiency that often presents with life-threatening hemophagocytic lymphohistiocytosis (HLH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance.
- NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_assertion evidence source_evidence_literature NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance.
- NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_assertion SIO_000772 19288545 NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance.
- NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_assertion wasDerivedFrom befree-2016 NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance.
- NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_assertion wasGeneratedBy ECO_0000203 NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance.
- befree-2016 importedOn "2016-02-19" NP726351.RAXVnc6nmUQGCEUTGiAfzJCYlLpWbyGq7TWgwgUCTfVcY130_provenance.